Canonical Allele Identifier: PA2828471993
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2938319
ClinVar RCV Id: RCV003797141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Cys1181Phe
CA1940133
NM_001371246.1:c.3542G>T